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A 2-Year-Old Girl with Acute Encephalopathy After Febrile Systemic Illness
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A 10-Year-Old Boy with Progressive Tremor, Insomnia and Autonomic Dysfunction
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Multivessel Cerebral Occlusion in Noonan Syndrome
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Melas Syndrome
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A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
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RNF213 Polymorphisms in Intracranial Artery Dissection
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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Neonatal Seizures
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Unilateral Leukoencephalopathy Revealing Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Imaging Patterns Characterizing Mitochondrial Leukodystrophies
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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Pediatric Leigh Syndrome
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Acute Cortical Lesions in MELAS Syndrome: Anatomic Distribution, Symmetry, and Evolution
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Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
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Bipolar II Disorder as the Initial Presentation of CADASIL:An Underdiagnosed Manifestation
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A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
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Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
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Characyeristic features and progression of abnormalities on MRI for CARASIL
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Red Papules on the Tongue of a Patient with Hemiparesis
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Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
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Conventional MRI and NOTCH3 Gene Screening in Sporadic CADASIL
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Genomewide Association Studies of Stroke
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Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study
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Decoding Cryptogenic Cardioembolism
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Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Series of 126 Patients
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Metabolic Disease and Stroke: MELAS
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Dystonia
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Familial Multiple Sclerosis and Other Inherited Disorders of the White Matter
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Hyperhomocysteinemia, Low Folate and Vitamin B12 Concentrations, and Methylene Tetrahydrofolate Reductase Mutation in Cerebral Venous Thrombosis
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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
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Autosomal Dominant Acute Necrotizing Encephalopathy
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New Players in the Genetics of Stroke
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Clinical Profile of Stroke in 900 Patients with Hypertrophic Cardiomyopathy
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Hypertrophic Cardiomyopathy A Systematic Review
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Advances in the Genetics of Cerebrovascular Disease and Stroke
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Impact of the Human Genome Projects and Identification of a Stroke Gene
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